In my current role I spend a lot of time on LinkedIn. A core task is to identify possible customers, and LinkedIn is rich hunting ground. I'm still sending each reach-out message individually (though admittedly often by pasting a message copied from a growing bank of crafted pitches), so even if I wasn't morally opposed to broad spamming I don't have the bandwidth for it. LinkedIn offers many ways for possible customers to reveal their interests - there's one's profile, any posts you make, comments on other posts, and what you hit like on. Indeed, those last two can be particularly valuable as LinkedIn has some constraints on search results based on my localization within the broad LinkedIn connection graph, comments plus likes are categories which can leap me away from my parochial bounds. Because I use LinkedIn so much, I of course have opinions about what I perceive as shortcomings, which I will periodically impose on the readers of this space. And today's is my frustration and degree of bewilderment that LinkedIn lacks an API.
Omics! Omics!
A computational biologist's personal views on new technologies & publications on genomics & proteomics and their impact on drug discovery
Friday, March 27, 2026
Monday, March 23, 2026
ElysION Fields
Even before new CEO Francis Van Parys took the reins at Oxford Nanopore with the start of the month, the company had made yet another priming to the instrument lineup. The sample-to-answer ElysION has been sent to its eternal rest, presumably in the nicer part of Hades
Image courtesy of Rasmus Kirkegaard
Tuesday, March 10, 2026
Roche Axelios1 Run Pricing: Not A Knockout - Yet?
By far the most awaited news at AGBT was Roche's reveal of the pricing scheme for Axelios 1 consumables: what would be the structure and how much would different runs cost? Indeed, Roche sequencing systems chief Mitu Chaudhary walked on to "The Final Countdown". Roche did show its hand here, but stayed coy on the launch schedule beyond "Summer 2026". Roche's pricing scheme clarified many questions, but also raised new ones.
Friday, March 06, 2026
Complete Genomics Sale: Gruyère or Emmental?
A bit of interesting news during AGBT was the announcement of the sale of Complete Genomics to Swiss Rockets, a Basel-based company which had last October licensed rights to Complete Genomic's CoolMPS technology for markets except Asia-Pacific. This move is clearly designed to try to extract Complete Genomics from being banned in the future in US markets due to its perceived ties, in the minds of US lawmakers and politicians, to the government of China. Swiss Rockets would acquire full rights to the CoolMPS technology in most markets and importantly the key personnel of Complete Genomics such as founder Rade Drmanac. Complete Genomics will remain the branding for Swiss Rockets' genomics business. So the question arises, will this be a deal which fixes Complete's issues in a manner as solid as a nice hunk of Gruyère, or will it be as full of holes as a delicious wedge of Emmental?
Thursday, March 05, 2026
Ultima Genomics Solaris 2.0: Greater Version, Smaller Beads, Lose A Box
Ultima Genomics announced the 2.0 version of their Solaris chemistry at AGBT. Perhaps the biggest splash here is that Solaris 2.0 relies on an isothermal amplification chemistry operating on smaller beads, making a path to higher numbers of reads per wafer and eliminating the separate (and very large) emulsion PCR instrument.
Friday, February 27, 2026
Element Previews High-Throughput VITARI
On the Thursday before AGBT, Element Biosciences unveiled their VITARI high throughput sequencer, expected to ship in the second half of this year. VITARI surprised much of the sequencing community, including this pundit, as it seemed as though Element was devoting their development efforts to their AVITI24 multi-omic spatial system - which they continue to evolve.
Wednesday, February 25, 2026
Illumina Constellation Becomes TruPath Genome
Illumina is rebranding their Constellation mapped read technology to TruPath Genome and launching it into the marketplace. Priced at $395 per genome, TruPath Genome was presented as being superior to true long read approaches for generating haplotype blocks and for resolving difficult genetic disease loci. TruPath Genome relies on on-flowcell tagmentation of long input molecules, meaning that library prep moves entirely to the flowcell. TruPath genome runs on new NovaSeq X C8 flowcells (8 lanes) or the new C2 flowcell (2 lanes), with one sample per lane.
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